Double functionalized haemocompatible silver nanoparticles control cell inflammatory homeostasis

Infection, trauma, and autoimmunity trigger tissue inflammation, often leading to pain and loss of function. Therefore, approaches to control inflammation based on nanotechnology principles are being developed in addition to available methods. The metal-based nanoparticles are particularly attractive due to the ease of synthesis, control over physicochemical properties, and facile surface modification with different types of molecules. Here, we report curcumin conjugated silver (Cur-Ag) nanoparticles synthesis, followed by their surface functionalization with isoniazid, tyrosine, and quercetin, leading to Cur-AgINH, Cur-AgTyr, and Cur-AgQrc nanoparticles, respectively. These nanoparticles possess radical scavenging capacity, haemocompatibility, and minimal cytotoxicity to macrophages. Furthermore, the nanoparticles inhibited the secretion of pro-inflammatory cytokines such as interleukin-6, tumor necrosis factor-α, and interleukin-1β from macrophages stimulated by lipopolysaccharide (LPS). The findings reveal that the careful design of surface corona of nanoparticles could be critical to increasing their efficacy in biomedical applications.


Introduction
Reactive oxygen species (ROS) are highly active, short-lived, small molecules, which are essential in signaling functions, and regulation of physiological activities (e.g., cell growth, differentiation, senescence, or apoptosis) in living cells. However, excessive production of ROS results in oxidative damage in cells/tissues, leading to the progression of inflammatory diseases [1,2]. Inflammation, per se, is a defensive mechanism triggered by infection and injury against foreign pathogens. While acute inflammation mainly involves prostaglandins, chronic inflammation entails numerous inflammatory cytokines, including IL-1 and TNF-α [1,3,4]. In addition, specific ROS species behave pro-inflammatory by activating c-Jun N-terminal kinase (JNK), protein kinase C, growth factor tyrosine kinase receptor, and extracellular signal-regulated kinase signaling pathways [3]. Clinically, inflammation is managed through non-steroidal anti-inflammatory drugs (NSAIDs) and glucocorticoids for acute and chronic inflammation. However, high dosages and prolonged use of these drugs have numerous side effects. Thus, it is imperative to find alternatives to the chronic and sole use of NSAIDs and glucocorticoids. In this context, plantderived phytochemicals are helpful because of their lower toxicity. However, adverse events may arise due to incorrect species of medicinal plants or dosing and interaction with other drugs. Therefore, alternative approaches for new anti-inflammatory agents with sustained release and better efficacy are sought. In this direction, nanotechnology offers promise in drug development with enhanced efficacy and controlled drug release.
In the past few decades, tremendous interest has been reported in biomedical research of metallic nanoparticles such as silver (Ag) and gold (Au). These can reduce oxidative stress through their efficient radical scavenging activities. Ag-based nanoparticles also confer a broad range of antimicrobial activity and are used in various wound dressings to control bacterial infections. They are also well known for anti-fungal, anti-inflammatory, and antioxidant activities [5,6]. Thus, Ag nanoparticles have contributed significantly to the field of biomedicine. However, the nanoparticle synthesis route is vital to extend their full potential, and hence it is crucial to develop monodispersed particles and fine-tune their physicochemical properties to reduce toxicity [7][8][9].
The biosynthetic methods involving phytochemicals enable novel opportunities in reducing Ag ions to form Ag nanoparticles. Alkaloids, flavonoids, and anthraquinones are natural active components of curcumin (Curcuma longa), a plant-based natural lipophilic compound [10]. Curcumin shows anti-inflammatory, antioxidant, anti-cancer, and anti-bacterial activities [11]. In addition, it targets various transcription factors and inhibits the production of proinflammatory cytokines, including interleukin 6/8 and TNF-α [12]. It is also an inducer of cell death via extrinsic and intrinsic apoptosis pathways and regulates gene expression [13]. However, curcumin's efficacy is limited because of its poor water solubility, low absorption, and rapid degradation. These problems can be surmounted by loading or conjugating curcumin on the surface of nanoparticles [14,15]. In addition, the release of hydrogen from curcumin shows a reduction of metal ions and thus acts precursor for nanoparticle formation [16], whereas nanoparticle's utility in biomedicine depends upon their surface modification with drugs, biomolecules, ligands, or amino acids [17][18][19][20][21][22].
In this study, we report curcumin-based Ag nanoparticles (Cur-Ag) synthesis, followed by their surface alteration with isonicotinic acid hydrazide (INH, isoniazid), tyrosine (Tyr, 4-hydroxyphenylalanine), and quercetin (Qrc, plant flavonol) to formulate Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles, respectively. These molecules were selected based on their potential biomedical capabilities. Thus, isoniazid is an antibiotic, tyrosine is an amino acid of biological origin, and quercetin is an antioxidant. Isoniazid is the first-line antibiotic used to treat Mycobacterium infection by inhibiting mycolic acid, a structural component of the Mycobacterium cell envelope. Isoniazid surface-modified particles can enhance the bioavailability of the drug in treating tuberculosis [23,24]. Conjugation of isoniazid with other molecules, including curcumin, can lower hepatotoxicity, improve stability, and enhance bioavailability [25].
Similarly, amino acid-based surface corona can offer a natural identity to nanoparticles. Thus, tyrosine is a proteinogenic amino acid [26], and its presence on the nanoparticle's surface can provide an additional biological identity to the particle. Moreover, due to the zwitterionic nature of amino acids, the surface charge of nanoparticles can be easily tailored by varying the solution pH [27,28]. Likewise, quercetin is vital for antioxidant, anti-cancer, antiinflammatory, and antiviral activities [29]. However, its poor water solubility, chemical instability, and low bioavailability limit the biomedical application of quercetin. To overcome these issues, modification, and further enhancement of efficacy in the nano-formulation-based system have been accomplished, and the nanoscale size material can facilitate their interaction with various biomolecules [30]. Hence, surface functionalization of Cur-Ag nanoparticles with isoniazid, tyrosine, and quercetin can provide unique opportunities to control the cell inflammatory haemostasis balance due to the involvement of diverse surface chemistries.
The Raw 264.7 macrophage cells from RIKEN cell bank of RIEKN cell engineering division, Tsukuba, Ibaraki, Japan; RNAiso reagents from Takara Biolabs, Tokyo, Japan. OxiSelect TM intracellular ROS assay Kit from Cell BioLabs, Inc, San Diego, CA, USA. Semi-quantitative PCR (q-PCR) by DreamTaq Green PCR master mix from Thermo Fisher Scientific, Waltham, MA, USA, and bicinchoninic acid (BCA) protein assay kits from Thermo Scientific, Carlsbad, USA. All the chemicals and reagents were used as received according to manufacturer instructions. Ultrapure milli-Q water was used throughout the study with a resistivity of 18.2 MO cm at 25˚C. All the glassware used to prepare nanoparticles were thoroughly washed with aquaregia (a mixture of concentrated HCI and HNO 3 ).

Curcumin-mediated synthesis of Ag nanoparticles and their surface functionalization
In a typical experiment, Cur-Ag nanoparticles were synthesized using curcumin as a reducing and stabilizing agent. First, in a 50 mL aqueous solution, 1 mM KOH and 0.25 mM curcumin were allowed to heat, followed by dropwise addition of 1 mM of AgNO 3 under constant stirring. After adding AgNO 3 (within 5-10 mins), a yellowish-brown color developed, indicating the formation of Cur-Ag nanoparticles. Next, to increase the metal content (2x) in the solution, Cur-Ag nanoparticles were subjected to slow heating with constant stirring. Additionally, the concentrated Cur-Ag nanoparticles solution was dialyzed using a dialysis membrane to remove the unreacted molecules and ions against Milli-Q water for 3 h at room temperature. Later, the concentrated, and dialyzed Cur-Ag nanoparticles, further surface functionalized with 0.25 mM of isoniazid, tyrosine, or quercetin to produce Cur-Ag INH , Cur-Ag Tyr, and Cur-Ag Qrc , respectively. After successful surface modification, these solutions were again subjected to dialysis to remove any unbound molecules from the surfaces against Milli-Q water.

Assessment of radical scavenging capacity (RSC) of nanoparticles
ABTS assay was performed to determine the RSC of nanoparticles. Three different concentrations of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles (0.0412 mmol/L, 0.0618 mmol/L, and 0.0824 mmol/L) were allowed to react with ABTS �+ . A decrease in the absorbance was measured at 734 nm to calculate the percentage RSC. ABTS �+ radicals were formed by reacting 7.4 mM of ABTS and 2.45 mM of potassium persulphate in the ratio of (2:1) by keeping them in the dark for 12-16 h at room temperature. The color change is an indication of radical formation. These pre-formed ABTS �+ radicals were further diluted to achieve an absorbance of 0.67±0.02 with absolute ethanol at 734 nm. The formed ABTS �+ radical cation is inhibited by the antioxidant nature of nanoparticles [31, 32].

Haemocompatibility of nanoparticles
The effects of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr, and Cur-Ag Qrc nanoparticles are assessed on red blood cells (RBCs) at 5 different concentrations of nanoparticles. The assay was performed using 5 mL of blood sample in a pre-EDTA stabilized tube and centrifuge at 10,000 rpm at 4˚C for 10 min to separate blood components by settling RBC at the bottom. Then, the supernatant was discarded, and the pellet with RBCs was resuspended in 0.9% sodium chloride (isotonic to RBC) to make a suspension. Next, the nanoparticles were treated with five different concentrations (0.00412 mmol/L, 0.0206 mmol/L, 0.0412 mmol/L, 0.0618 mmol/L, and 0.0824 mmol/L) of nanoparticles with 2.1 mL of diluted RBC suspension and incubated for 3 h on a shaker at room temperature. After incubation, centrifugation was carried out at 10,000 rpm/3 min, and the haem release in the supernatant was measured at 540 nm to calculate the percentage of haemolysis. The same treatment was also given to positive and negative controls by taking 1% SDS and 0.9% sodium chloride with the respective volume of RBC suspension.

MTT assay
Cell proliferation of mouse Raw 264.7 macrophages was evaluated using MTT assay. The assay was performed by having cells from early (3-4) passage and cultured in Dulbecco's modified Eagle low glucose medium with 10% heat-inactivated fetal bovine serum and antibiotic combination including (5 mg/mL penicillin, 5 mg/mL streptomycin, and 10 mg/mL neomycin) at 37˚C with 5% CO 2 . Semi confluent cells (1x10 4 cells/mL) were seeded and treated with different concentration 0.00 mmol/L, 0.0011 mmol/L, 0.0027 mmol/L, 0.0054 mmol/L, and 0.0082 mmol/L of nanoparticles and further incubated for the standard time of 16 h. The intracellular purple formazan was quantified with a UV-Vis spectrophotometer at an absorbance of 570 nm.

Intracellular ROS detection by fluorescence microscopy
The generation of intracellular ROS was measured by fluorescence microscopic method using the intracellular ROS assay Kit. 1x10 3 cells/mL of mouse RAW 264.7 macrophages were seeded onto the culture suitable coverslips and treated with different nanoparticles for 16 h under a typical cell culture procedure. Following the treatment, 10 μM of 2'-7'-Dichlorofluorescin diacetate (DCFH-DA) was added at 37˚C for 1 h. After treatment with DCFH-DA, cells were fixed with 4% paraformaldehyde and mounted on the cover glass. The degree of green-fluorescent intensity was observed at 20x under a confocal laser scanning microscope.

Cytokine expression assays
Semi-confluent Raw 264.7 macrophages were treated with 1 μg/mL of LPS with or without different test nanoparticles (Cur-Ag, and Cur-Ag Tyr , 0.0054 mmol/L at 24 h; Cur-Ag INH , and Cur-Ag Qrc , 0.0054 mmol/L at 12 h, and 16 h). After the treatment, total RNA was isolated using RNAiso reagents, and the first strand of cDNA was prepared. The transcript levels of the gene of interest were measured by semi-quantitative PCR (q-PCR) using the DreamTaq Green PCR master mix. Further, PCR products were electrophoresed on 1% agarose gel, and resulting bands were detected using the Bio-Rad digital imaging system. Band intensity was analyzed by ImageQuant TL software. β-actin was used as a housekeeping gene to normalize the individual inflammatory gene.
Following primers were used in the study of the inflammatory genes: The mRNA expression profiles were further corroborated by Western blotting. Briefly, macrophages treated with LPS, and nanoparticles were lysed with cold RIPA cell lysis buffer, and a BCA protein assay kit was used to determine protein concentrations, followed by resolving 10 μg protein in 17% SDS-PAGE gels. Later, the separated protein was transferred to the PVDF membrane and blocked (blotted membrane) for 1 h after incubation with primary antibodies (anti-rabbit IL-6, anti-rabbit TNF-α, anti-rabbit IL-1β, anti-rabbit β-actin) at room temperature. In the end, these were probed with HRP conjugated secondary antibody (after washing with T-TBS membranes), and immunoreactivity of protein expression was detected.

Statistical analysis
One-way and two-way ANOVA (analysis of variance) with Tukey's post-test analysis were used for statistical comparisons using the GraphPad Prism™ software (San Diego, CA; Version 5.0). Data are expressed as mean ± SE or mean ± SD. Unless specified otherwise, all experiments were performed in triplicates.

Results and discussion
As illustrated in Fig 1, the present work focuses on preparing Ag nanoparticles with an aqueous solution of curcumin (reducing and stabilizing agent) and AgNO 3 under an alkaline environment. After preparing Cur-Ag nanoparticles, they were functionalized using isoniazid, tyrosine, and quercetin to generate Cur-Ag INH , Cur-Ag Tyr, or Cur-Ag Qrc nanoparticles, respectively.
Curcumin (Cur) has three important functional groups, an aromatic methoxy phenolic group, α, β-unsaturated β-diketo linker, and keto-enol tautomerism. The keto and the phenolic groups are involved in H-bonding [33]. In an alkaline pH environment, the phenolate and enolate anions of curcumin help reduce Ag + ions, thus producing Cur-Ag nanoparticles. Furthermore, at the alkaline pH, the nanoparticles formed show a high dispersity facilitated by a higher number of Ag(I) binding [34]. Next, surface functionalization was performed with isoniazid, tyrosine, and quercetin to obtain Cur-Ag INH , Cur-Ag Tyr, or Cur-Ag Qrc nanoparticles. The molecules for functionalization were selected based on their unique properties. Oxidized isoniazid, under alkaline pH conditions, binds on the surface of Cur-Ag nanoparticles as carboxylic acid binds to Ag [23,24]. In tyrosine, the phenolic group gets converted into the semiquinone group and acts preferred site of binding on Cur-Ag nanoparticles [35,36]. In addition, tyrosine's aromatic moiety, C = O, and -NH 2 functional groups are involved in binding. This binding interaction is mediated through the C = O of curcumin and the NH 2 group of tyrosine [37]. Moreover, the aqueous solution has alkaline pH well above the isoelectric point of tyrosine (PI~5.66), indicating the overall negative surface charge, which was confirmed by zeta potential values [28]. In quercetin, the presence of phenolic group and Hdonating ability promotes reduction. In the reduced form, the OH groups convert into the carbonyl group (C = O). These C = O groups in the oxidized form of polyphenol electrostatically stabilize the metal nanoparticles [38] and can attach to the surface of Cur-Ag nanoparticles to form Cur-Ag Qrc nanoparticles. The chemical reactions for binding of tyrosine, isoniazid, and quercetin on the surface of Cur-Ag nanoparticles are shown in Fig 2D.  Fig 2A and 2B demonstrate the absorption spectra, optical images of nanoparticle solutions, and TEM micrographs of synthesized Cur-Ag and subsequent surface-functionalized Cur-Ag INH , Cur-Ag Tyr, and Cur-Ag Qrc nanoparticles. A good color change is an indication of AgNPs formation. The color changed from colorless to pale yellow at the start of curcumin, which intensified as the reaction proceeded and subsequently changed to yellow-brown with time, suggesting the development of Cur-Ag nanoparticles. This color change indicates the excitation of metal nanoparticle surface plasmon vibration [39]. In addition, variation in color intensity was observed from Cur-Ag nanoparticles to Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles indicating successful functionalization (Fig 2B).
Further, UV-visible spectroscopy was performed to confirm the synthesis and stability of nanoparticles in aqueous solutions. Cur-Ag nanoparticles gave surface plasmon resonance (SPR) at~428 nm due to the π!π � transition, and an additional band at~262 nm was also observed due to the n!π � transition from carbonyl and hydroxyl group [40,41]. After surface modification of Cur-Ag nanoparticles with isoniazid, the SPR band red-shifted to~432 nm. Similarly, the functionalization of Cur-Ag with tyrosine shifted the SPR to~430 nm. However, when Cur-Ag nanoparticles are functionalized with quercetin, the values remain unchanged at 428 nm, which might be due to the strong binding interactions of curcumin and quercetin molecules (Fig 2A). Similarly, as shown in S1 Fig in S1 File, the pyridine group of pure isoniazid exhibits an absorption band at~262 nm due to π!π � transition [24], and the pristine tyrosine indicates an absorption band at~224 nm owing to π!π � transitions of the peptide bonds [42], and quercetin at~264 nm due to π!π � electronic transition of aromatic chromophore [43]. Finally, the TEM analysis was carried out to determine the morphology of nanoparticles, as shown in Fig 2B(a-d). All the Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles are spherical to quasi-spherical in shapes with higher monodispersity. Moreover, there were no visible signs of aggregation in any of the nanoparticles solutions, indicating the stability of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles, and it was confirmed employing zeta (z-) potential measurements of the nanoparticles.
As shown in Table 1, the zeta (z) -potential and DLS measurements were applied to assess the surface charge and hydrodynamic radii (R hyd ) of synthesized Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles. The effective surface charge and hydrodynamic radius of nanoparticles play a central role in determining the aggregation states of nanoparticles. Cur-Ag nanoparticles showed z-potential values of -26.5 mV, which further changed after their surface functionalization. For Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles, the effective z-potential values are found to be -26.7 mV, -28.4 mV, and -25.1 mV, correspondingly ( Table 1). The reported high negative z-potential values of the nanoparticles are responsible for electrostatic repulsion between the nanoparticles, and that is why these nanoparticles are highly stable [34]. The DLS studies confirmed the hydrodynamic size of nanoparticles, which was found to be 23.83 nm, 30.13 nm, 30.32 nm, and 32.71 nm for Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles, respectively. The hydrodynamic size of Cur-Ag INH , Cur-  Further, FTIR was employed to identify the presence of different functional groups on the surface of nanoparticles and to confirm the capping of curcumin, isoniazid, tyrosine, or quercetin molecules on nanoparticles (Fig 2C). As shown in S2 Fig and S1 Table in S1 File, the curcumin shows vibrational frequencies at~1272 cm -1 ,~1636 cm -1 , and~2114 cm -1 . Due to the C-O stretching of the phenolic group, C = O stretching of conjugated ketone, and symmetric vibration of the CH 3 group [44]. Likewise, pristine isoniazid (S2 Fig in S1 File) exhibited its unique vibrational frequencies at~1435 cm -1 due to C-N stretching or -NH bending,~1634 cm -1 for C = O stretching,~1216 cm -1 due to C-OH (phenolic OH) stretching,~1228 cm -1 because of N-N single bond,~1417 cm -1 due to pyridine ring,~1488 cm -1 for N-O stretching, and~1557 cm -1 due to N-H bending [45]. In tyrosine, the frequencies are found to be at 1217 cm -1 ,~1229 cm -1 ,~1558 cm -1 ,~1633 cm -1 , and~1737 cm -1 originating from the C-OH (phenolic) stretching, N-N single bond, N-H bending, carbonyl stretching vibration from the carboxylate ion, and C = O stretching mode, respectively [46,47]. Similarly, for quercetin molecule show its fundamental vibrational frequencies at~1170 cm -1 ,~1229 cm -1 or~1267 cm -1 , and~1525 cm -1 assigned to stretching of the benzene ring, C-O stretch of phenolic OH (-C-O-H) group and C = C stretching. All the nanoparticles (Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc ) reveal distinctive vibrational frequencies with some changes for curcumin, isoniazid, tyrosine, or quercetin molecules on individual nanoparticles, which confirms the presence of the corresponding molecule on the surface of Ag nanoparticles. All the critical vibrational frequencies and the groups they originate from are shown in S1 Table in S1 File for all the nanoparticles.
After confirming the physicochemical characteristics of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles, they were subjected to investigate their potential biological properties, including %RSC, haemocompatibility, and cell viability/anti-inflammatory effects using mouse Raw 264.7 macrophages.
The ABTS assay is one of the most widely used synthetic radical assays for estimating antioxidant activity. ABTS is first oxidized by potassium persulphate to generate cation radicals of ABTS .+ , which are formed by emitting one electron from the nitrogen atom. The produced blue-green color of radicals can be measured spectroscopically at 734 nm. The ABTS .+ reacts with antioxidant molecules leading to the decolorization of the solution, and the calculated % RSC is directly related to the antioxidant activity of the compounds [48,49]. RSC of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles was tested at three different doses 0.0412 mmol/L, 0.0618 mmol/L, and 0.0824 mmol/L, as shown in Fig 3A. Cur-Ag nanoparticles show antioxidant behavior like the study reported earlier. The antioxidant nature is derived from the hydrogen in the phenolic or central methylene groups [50,51]. Post-functionalization leads to an increase in activity for Cur-Ag INH , Cur-Ag Tyr , or Cur-Ag Qrc nanoparticles. The order of increasing activity was Cur-Ag Qrc > Cur-Ag INH > Cur-Ag Tyr > Cur-Ag nanoparticles. The maximum activity of Cur-Ag Qrc nanoparticles is due to their excellent antioxidant nature, which strongly influences scavenging of free radicals by donating hydrogen atoms or an electron to the free radicals [52]. The antioxidant activity of the flavonoids depends on their functional group arrangement [53] on the surface of nanoparticles. A comparison of 0.0618 mmol/ L Ag concentration of all the nanoparticles with the statistical analysis is also shown in Fig 3A, which indicates the significant %RSC of Cur-Ag Qrc nanoparticles (p<0.0001). In similar experimental conditions, curcumin, isoniazid, tyrosine, quercetin, and AgNO 3 were also tested for their RSC, as displayed in S3 Fig in S1 File. The isoniazid showed negative values indicating a negative impact on the RSC due to inducing free radicals, which then exert toxicity to the cells. However, free AgNO 3 , curcumin, tyrosine, and quercetin have shown RSC activity because of their inherent nature, and the activity of these molecules was found to be lesser than those of synthesized nanoparticles [54][55][56].
Nanoparticle exposure can lead to cellular injuries, nucleic acid damage, cardiovascular diseases, and anemia [57,58]. In the body, blood is the most common circulating fluid; hence, nanoparticle exposure is inevitable [59]. Thus, it is essential to evaluate the probable toxic effects of synthesized nanoparticles on RBCs. In this context, nanoparticles' different sizes and dose-dependent activity have been evaluated for toxicity toward blood [57]. Further, it has been established that using different capping and stabilizing agents can reduce nanoparticles' toxicity [60]. Furthermore, the rupturing of RBCs after nanoparticle treatment can release its internal component into the surrounding fluid that can be visually detected by showing a red color [61]. Therefore, a haemocompatibility assay was performed to evaluate the toxic effects of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles on RBCsby selecting four different concentrations: 0.00412 mmol/L, 0.0206 mmol/L, 0.0412 mmol/L, 0.0618 mmol/L, and 0.0824 mmol/L (Fig 3B). The %haemolysis increased with the concentration of nanoparticles in a dose-dependent manner (p < 0.05). Whereas a comparison of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles at 0.0618 mmol/L Ag concentration shows significantly higher haemolysis for Cur-Ag INH and Cur-Ag Qrc with respect to pristine Cur-Ag nanoparticles (p>0.9999). However, it is important to state that less than 5% haemolysis was observed at all the evaluated concentrations, confirming the haemocompatibility of the Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles. Similarly, the effects of pristine AgNO 3 , curcumin, isoniazid, tyrosine, and quercetin were also assessed on RBCs (S4 Fig in S1 File).
Further, cell viability studies were conducted on mouse Raw 264.7 macrophages to evaluate the toxic effects of nanoparticles on cells. The MTT assay was performed to assess the cell viability dose-dependent for all the synthesized nanoparticles. The MTT assay is based on the conversion ability of yellow tetrazolium MTT salt into blue MTT formazan crystals by the mitochondrial succinate dehydrogenase enzyme of living cells. Viable cells take up the dye and pass it into mitochondria, which are then solubilized to release MTT formazan, and it can be measured spectrophotometrically at 570 nm to confirm viability [62,63]. As shown in Fig 3C, the assay performed on mouse Raw 264.7 macrophages using different concentrations 0.00 mmol/L, 0.0011 mmol/L, 0.0027 mmol/L, 0.0054 mmol/L, and 0.0082 mmol/L of respective nanoparticles. For the concentration of 0.00 mmol/L, the viability is considered to be 100%. The viability seems to be varied with the surface modification. Cur-Ag nanoparticles at 0.0011 mmol/L concentration showed~100% viability, which drops significantly to~79%,~69%, and 40% with the increasing doses. Cur-Ag INH and Cur-Ag Tyr nanoparticles demonstrated good cell viability at all the evaluated doses. The Cur-Ag Qrc nanoparticles indicated the highest viability (p<0.0001), and at 0 the upper evaluated dose 0.0082 mmol/L, it shows over~200% cell viability, which may be attributed to the quercetin surface corona. The results demonstrate the nanoparticles' biocompatibility and the importance of their surface functionalization.
Nevertheless, it has been reported that Ag nanoparticles can induce toxic effects on cells by inhibiting cell growth, cell morphology changes, and ROS production [64]. These ROS underlie oxidative stress, which damages the intracellular structures, including mitochondria, and DNA ribosomes, ultimately leading to cell death [65,66]. Therefore, to further assess the effect of nanoparticles' potential toxicity on different organelles via ROS production, in vitro DCFH-DA assay was performed [67]. DCFH-DA is taken up by the cells, and the presence of the cellular esterase cleaves the acetyl groups, leading to the form of DCFH. Further oxidation of DCFH by ROS converts the molecule to DCF, which emits green fluorescence at an excitation wavelength of 485 nm, and an emission wavelength of 530 nm [68]. The effects of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles of 0.0054 mmol/L concentration were assessed on mouse Raw 264.7 macrophages, as shown in Fig 3D. The treatment of Cur-Ag, Cur-Ag Qrc , and Cur-Ag Tyr nanoparticles showed mild emission of green fluorescence when co-treated with lipopolysaccharides (LPS).
In contrast, Cur-Ag INH nanoparticles show some fluorescence, indicating that the formulated Cur-Ag, Cur-Ag Qrc, and Cur-Ag Tyr nanoparticles are nontoxic to the internal organelles and provide a protective effect to LPS-treated macrophages (Fig 3D). However, LPS-Cur-Ag INH nanoparticles showed slight fluorescence compared to all other LPS co-treated nanoparticles, indicating their lesser protective impact, which can be attributed to the antibiotic surface corona of nanoparticles. The relative fluorescence intensity of these nanoparticles cotreated with LPS is also evaluated (Fig 3E), and from the results, it can be concluded that the low impact of nanoparticles on the cells can be attributed to their specific surface biomolecules.
Besides cell death, the nanoparticles have been shown to enhance the expression of proinflammatory cytokines and activate inflammatory cells, which further increase the generation of ROS in cells [69]. Therefore, the production of pro-inflammatory IL-6, IL-1β, and TNF-α cytokines by co-treatment of 0.0054 mmol/L of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles with LPS is assessed. LPS is well known to stimulate the production of pro-inflammatory IL-6, IL-1β, and TNF-α. As illustrated in Fig 4, the treatment of mouse 264.7 macrophages with LPS increased the transcription of pro-inflammatory genes. However, the co-treatment of macrophages with Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , or Cur-Ag Qrc nanoparticles caused a significant decrease in the transcription of pro-inflammatory cytokines especially for IL-6. Moreover, the Western blotting was performed for the similar concentrations of Cur-Ag, Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles as shown in Fig 5. Herein, it is essential to state that the β-actin was used as a housekeeping gene to assess macrophage inflammatory response (Figs 4 and 5).
The expression of pro-inflammatory cytokines protein expression increased with the treatment of LPS. However, co-treatment with the nanoparticles significantly reduced (p<0.0001) the expression of pro-inflammatory cytokine TNF-αas shown in (Fig 5A). This can be attributed to the presence of curcumin, isoniazid, tyrosine, or quercetin biomolecules helps in reduction of pro-inflammatory cytokines (IL-6, IL-1β, and TNF-α). To further validate the observations, pure curcumin, isoniazid, tyrosine, and quercetin molecules were employed in similar experimental conditions, as shown in S5 and S6 Figs in S1 File. From Figs 4 and 5, it can be clearly concluded that the different surface coronas of the nanoparticles can influence different genes and accordingly up or down-regulate the cytokines expression. In addition, the Ag nanoparticles are reported to have anti-bacterial, anti-fungal, and immunomodulatory activities [70][71][72].
In contrast, curcumin shows anti-inflammatory action due to the presence of keto form and a double bond in the structure leading to controlling various transcription factors, cytokines, and protein kinases [73]. Moreover, curcumin inhibits the synthesis of inflammatory molecules like TNF-α, which is responsible for producing inflammatory products. It modulates the inflammatory response by down-regulating the expression of cyclooxygenase-2 (COX-2), lipoxygenase (LOX), and phospholipase A2 (PLA2s) enzyme pathway that hinders the inflammatory response mediators [74,75]. Likewise, free quercetin inhibits the production of TNF-α and nitric oxide (NO) in murine macrophages [76]. The findings confirm that the double functionalized nanoparticles can down-regulate pro-inflammatory genes. By choosing specific biomolecules and nanoparticles, the biomedical potential of the particles can be finetuned, and new prospects in nanomedicine can be achieved.

Conclusion
Hitherto, silver nanoparticles have been used for their anti-bacterial potential, whereas curcumin is a naturally occurring traditional therapeutic agent. However, due to the water-insoluble nature, the full therapeutic benefits of curcumin have not been realized. Recent developments in nanotechnology and the essential role of surface corona wherein organic-inorganic moieties can be conjugated can open new avenues for biology and medicine. Therefore, in the present study, Cur-Ag nanoparticles are synthesized, and a suitable surface corona of isoniazid, tyrosine, and quercetin is engineered around them to develop Cur-Ag INH , Cur-Ag Tyr , and Cur-Ag Qrc nanoparticles. The impact of the dual surface corona containing curcumin and a functional biomolecule has been evaluated by different in vitro biological assays. The interaction of nanoparticles with RBCs, mouse RAW 264.7 macrophages, and pro-inflammatory cytokines confirm their haemocompatibility, cytocompatibility, and anti-inflammatory properties. Among the Cur-Ag, Cur-Ag INH , Cur-Ag Tyr, and Cur-Ag Qrc nanoparticles, Cur-Ag Qrc nanoparticles showed relatively higher radical scavenging capacity, positive impact on cell viability and cell proliferation, and lesser generation of reactive oxygen species. Furthermore, the specific surface corona on nanoparticles can influence different genes and accordingly up or down-regulate cytokine expression to control inflammation. The present study indicates the importance of engineered nanoparticle surfaces to unravel their innovative potential for nanomedicine applications. However, additional in vivo and experimental model studies must be conducted for further use of such functional nanoparticle systems.